NA 04.112.814SRecalls & reported problems
Synthes GmbH · 2.7MM TI VA LCP HOOK PLATE LONG/ 15MM/ LEFT/ STERILE · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982279675), received between Feb 19, 2026 and Feb 19, 2026 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Discomfort1
- Pain1
- Skin Inflammation/ Irritation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 19, 2026Adverse Event Without Identified Device or Use Problem
SUBJECT ID: (B)(6). STUDY NO: NO INFORMATION PROVIDED. DATE OF EVENT: 3 DEC 2025. DATE OF IMPLANT: (B)(6) 2025. DEVICE LOCATION: LEFT. ¿ POSTOPERATIVE ADVERSE EVENT: "PAIN/DISCOMFORT/PROMINENCE". ¿ IS THE AE RELATED TO THE IMPLANTATION OR EXPLANTATION OF THE HOOK PLATE? "POSSIBLE". ¿ IS THE AE RELATED TO THE INVESTIGATIONAL DEVICE (VA CLAVICLE PLATE/VA CLAVICLE HOOK PLATE)? " POSSIBLE". ¿ IS THE AE RELATED TO THE CONDITION UNDER INVESTIGATION? ¿POSSIBLE¿. ¿ DPS IMPLANT WAS USED. DEVICE RELATED: POSSIBLE. PROCEDURE RELATED: POSSIBLE. DEVICE LOCATION: LEFT. TREATMENT: IMPLANT REMOVAL, THE EVENT RESULTED IN A MEDICAL OR SURGICAL INTERVENTION TO PREVENT LIFE THREATENING ILLNESS OR INJURY OR PERMANENT IMPAIRMENT TO A BODY STRUCTURE OR A BODY FUNCTION. DEPUY SYNTHES PRODUCTS USED: CATALOG NUMBER: 04.112.814S. LOT NUMBER: NO INFORMATION PROVIDED. COMPONENT TYPE: PLATE. DESCRIPTION: 2.7MM TI VA LCP HOOK PLATE LONG/ 15MM/ LEFT/ STERILE. CATALOG NUMBER: 04.211.014TS. LOT NUMBER: NO INFORMATION AVAILABLE. COMPONENT TYPE: SCREW. DESCRIPTION: VA LOCKSCR ø2.7 HE 2.4 SELF-TAP L14 TAN. CATALOG NUMBER: 04.211.014TS. LOT NUMBER: NO INFORMATION AVAILABLE. COMPONENT TYPE: SCREW. DESCRIPTION: VA LOCKS
Patient problems: Discomfort; Pain; Skin Inflammation/ Irritation
MAUDE report 24388040 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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